Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47720 | A09 | 51858218 | G | A | missense_variant | MODERATE | c.1553C>T|p.Thr518Ile |
S265 |
2 | BAA09g47720 | A09 | 51859224 | C | T | missense_variant | MODERATE | c.656G>A|p.Arg219Gln |
S297 |
3 | BAA09g47720 | A09 | 51859682 | G | A | synonymous_variant | LOW | c.198C>T|p.Leu66Leu |
S264 |
4 | BAA09g47720 | A09 | 51860851 | C | T | upstream_gene_variant | MODIFIER | c.-972G>A| |
S130 S60 |
5 | BAA09g47720 | A09 | 51862510 | G | A | upstream_gene_variant | MODIFIER | c.-2631C>T| |
S239 |
6 | BAA09g47720 | A09 | 51864078 | G | A | upstream_gene_variant | MODIFIER | c.-4199C>T| |
S244 |
7 | BAA09g47720 | A09 | 51864081 | G | A | upstream_gene_variant | MODIFIER | c.-4202C>T| |
S129 |